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User Evaluation of the Peristomal Skin Condition in Ostomates Using ConvaTec Moldable Technology™

NCT02499588 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 600

Last updated 2015-07-16

No results posted yet for this study

Summary

The primary aim of this study is to demonstrate the maintenance of healthy peri-stomal skin over a two month period in subjects who use ConvaTec Moldable Technology™ Skin Barriers as part of their standard protocol of care following surgery.

Conditions

  • Colostomy
  • Ileostomy
  • Urostomy

Interventions

DEVICE

Esteem Plus with ConvaTec Moldable Technology

DEVICE

Natura with ConvaTec Moldable Technology

DEVICE

Natura Accordion with ConvaTec Moldable Technology

DEVICE

Esteem synergy Plus with ConvaTec Moldable Technology

Sponsors & Collaborators

  • ConvaTec Inc.

    lead INDUSTRY

Principal Investigators

  • Kim Peters, BSc (Hons) · Sponsor GmbH

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-06-30
Primary Completion
2016-08-31

Countries

  • Poland

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02499588 on ClinicalTrials.gov